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NCT ID: NCT03776240 Completed - Healthy Volunteers Clinical Trials

A Study to Demonstrate the Equivalent Pharmacokinetic Properties of a Single Intravenous Dose of HD201 and EU-Herceptin® and US-Herceptin® in Healthy Male Subjects

TROIKA-1
Start date: April 1, 2019
Phase: Phase 1
Study type: Interventional

The purpose of the study is to demonstrate demonstrate the pharmacokinetic (PK) similarity of HD201 to the European (EU) and American (US) reference products Herceptin, following a single i.v. infusion of 6 mg/kg in healthy volunteers.

NCT ID: NCT03780621 Completed - Clinical trials for Cognitive Impairment, Mild

Effects of an Adaptogenic Extract on Electrical Activity of the Brain in Elderly Subjects With Cognitive Impairment

Start date: April 1, 2019
Phase: Phase 1
Study type: Interventional

A randomized, double-blind, placebo-controlled, two arm cross-over study to determine whether a specific combination of Andrographis paniculata and Withania somnifera can be regarded as a safe and effective treatment for cognitive deficits.

NCT ID: NCT03781453 Completed - Health Behavior Clinical Trials

POWERPLAY Phase 2: Development and Evaluation in Male-dominated Workplaces

Start date: April 1, 2019
Phase: N/A
Study type: Interventional

With funding from the Alberta Ministry of Labour (Grant #095244772), a program called POWERPLAY (www.powerplayatwork.com), designed to promote men's health at work, will be evaluated in workplaces in Alberta.

NCT ID: NCT03786029 Completed - Tooth Extraction Clinical Trials

Pre-emptive Analgesic Administration in Primary Tooth Extraction

Start date: April 1, 2019
Phase: Phase 2/Phase 3
Study type: Interventional

Brief Summary: Aims: The objective of the current study will be to compare the effectiveness of Ibuprofen, Acetaminophen, and Placebo on reducing injection pain and post-operative pain in primary tooth extraction, and to compare the parents' satisfaction. Design: This will be a blinded, randomized placebo-controlled trial including sixty six cooperative children, aged 6-8 years old.

NCT ID: NCT03786627 Completed - Instability; Back Clinical Trials

Neuromuscular Electrical Stimulation and Motor Control

Start date: April 1, 2019
Phase: N/A
Study type: Interventional

Phase I, this study aims to:- 1. Establish intra- and inter-rater reliability and minimal detectable change of ultrasound imaging measurement 2. Determine appropriate mode and dose for neuromuscular electrical stimulation on lumbar multifidus muscle 3. Determine feasibility of proposed protocol and physical therapy intervention Phase II, this study aims to:- 1. Determine the difference lumbar multifidus muscle activation based on arthrogenic muscle inhibition model between individuals with and without impaired lumbopelvic control 2. Determine the effect of combined neuromuscular electrical stimulation and motor control training in individual with impaired lumbopelvic control

NCT ID: NCT03787121 Completed - Thyroid Cancer Clinical Trials

Estimation of Economic Consequences Linked With Different Care Management Pathways of Differentiated Thyroid Cancers

ECO-THYR
Start date: April 1, 2019
Phase:
Study type: Observational

The incidence of Thyroid Cancer (TC) has increased over the last thirty years, in France and worldwide. This increase is mainly due to good prognosis microPapillary TC (mPTC). Sixty percent of diagnosed cancers are considered as over-diagnosed, leading to an over-treatment of these cases. The increase of diagnosis of mPTC and its treatment inevitably leads to an increase of medical resources consumption and corresponding costs. The primary aim of this study is to estimate the cost related to different care management pathway of TC patient during a lifetime period using a multi-state Markov model. This is a retrospective, observational population based cohort study, using data from a cohort study of TC patients implemented by the ONCOMIP network which initially aimed to perform an audit of clinical practices for the management of TC, and from database of the French social health insurance of Midi-Pyrenees region to calculate observed costs of TC management during 24 months.

NCT ID: NCT03792737 Completed - Sutures Clinical Trials

A Study of Two Types of Absorbable Surgical Sutures in the Suturing of Thyroid Surgery Incision

Nautilus
Start date: April 1, 2019
Phase: N/A
Study type: Interventional

The primary objective of this study is to evaluate the efficacy and safety of two types of absorbable surgical sutures -- STRATAFIX Spiral PDS Knotless Plus Tissue Control Device and STRATAFIX Spiral MONOCRYL Plus Knotless Tissue Control Device (hereinafter referred to as Spiral PDS Plus and Spiral MONOCRYL Plus) used in thyroid surgery to suture surgical incision.

NCT ID: NCT03792802 Completed - Appendicitis Clinical Trials

EFFECT OF USING SAME DERMATOME LİNE FOR ALL PORT SİTES IN LAPAROSCOPIC APPENDECTOMY IN ACUTE APANDICITIS

DERMATOME
Start date: April 1, 2019
Phase: N/A
Study type: Interventional

Acute apandicitis is the one of most common cause of abdominal pain.Most of center still use open appendectomy(OA) technic for acute apandisitis.But Semm was defined Laparoskopic appendectomy(LA) with 3 ports in 1983.Today surgeons skill and experience ara increasing about LA day by day. Because of advantages of LA , this technical tend to be gold standart in acute apandisitis. In LA , all of centers use same technic as 3 ports for the surgery. Port sites located 1 infraumbilical , 1 right lower quadrant and 1 left lower quadrent in this surgery. But 3 dermatome lines have been effected in this style of location .This 3 points causes more pain postoperatively.In our study we will define the port locations into the same dermatome line (T10) . Purpose of this research is incerasing the postoperative pain score ,decreasing postoperative need of analgesia and develop the patient satisfy.

NCT ID: NCT03794089 Completed - Anxiety Clinical Trials

Reducing Anxiety and Stress in Primary Care Patients

Start date: April 1, 2019
Phase: N/A
Study type: Interventional

Anxiety is common among primary care patients, but is undertreated. The purpose of this study is to evaluate whether a brief anxiety treatment designed for VA primary care is more effective at reducing anxiety symptoms in Veterans compared to usual care. The investigators will also examine whether Veterans like the brief treatment and whether the treatment can be feasibly delivered in primary care. Forty-eight adult Veteran primary care patients from the Syracuse VAMC who are experiencing anxiety symptoms will be recruited and randomly assigned to receive the brief anxiety treatment or usual care. The brief treatment consists of up to six 30-minute sessions with a cognitive-behavioral skills focus. The investigators will compare anxiety symptom severity between the two groups at baseline and at post-assessment 16 weeks later.

NCT ID: NCT03794765 Completed - Ulcerative Colitis Clinical Trials

Antibiotics as an Adjuvant in Patients With Acute Severe Ulcerative Colitis

AAASUC
Start date: April 1, 2019
Phase: Phase 2
Study type: Interventional

The study is planned as a randomised control trial to study the adjuvant use of antibiotics (ceftriaxone and metronidazole) to achieve a clinical response in hospitalised patients with acute severe ulcerative colitis